Fluorinated oxygen-containing products and process for preparation thereof

ABSTRACT

Perfluorinated cyclic ethers and fluorinated linear polyethers. Prepared by photochemical reaction in liquid phase of perfluoropropylene with oxygen in presence of ultraviolet radiation.

United States Patent Sianesi et al;

[ F LUORINATED OXYGEN- CONTAINING PRODUCTS AND PROCESS FOR PREPARATION THEREOF [72] Inventors: Dario Sianesi; Adolfo Pasetti;

Costante Corti, all of Milan, Italy [73] Assignee: Montecatini Edison S.p.A Milan,

Italy 22 Filed: May 1, 1970 21 Appl.N0.:.31,852

Related us. Application Data [63] Continuation of Ser. No. 650,257, June. 30,

1967, abandoned, which is a.continuation-inpart of Ser. No. 446,292, April 7, 1965, Pat. No. 3,442,942.

[30] A .Foreign Application Priority Data July 6, 1966 Dec. 16, 1966 Italy ..3ll93 A/66 Italy ..15625 A/66 [52] U.S. Cl. ..'.....2 60/463, 204/158, 260/340.9, I

1 Primary Examiner-Alex Mazel Assistant Examiner.lames H. Turnipseed Attorney-Hubbell, Cohen & Stiefel [57 ABSTRACT,

Perfluorinated cyclic ethers and fluorinated linear polyethers. Prepared by photochemical reaction in liquid phase of perfluoropr'opylene with oxygen in presence of ultraviolet radiation.

5 Claims, No Drawings Bleu et al... 260/544- FLUORINATED OXYGEN-CONTAINING PRODUCTS AND PROCESS FOR PREPARATION THEREOF CROSS REFERENCE TO RELATED APPLICATION This application is a continuation of copending application Ser. No. 650,257, filed June 30, 1967, now abandoned, which application is in turn a continuationin-part application of our U.S. patent application Ser. No. 446,292 filed Apr. '7, 1965 now US. Pat. No. 3,442,942 issued Apr. 7, 1969.

BACKGROUND OF THE INVENTION l. Field of the Invention This invention-relates to new products consisting essentially of carbon, fluorine and oxygen atoms having the structure of linear polyethers or of cyclicethers, to a process for, preparation thereof, and to anew method for the preparation of epoxide of perfluoropropylene, COF and CF COF. v

. Chemical resistance and thermal resistance are two of the most attractive and appreciated characteristics For other applications, e.g., for use as fluids for heat transfer, for lubrication underparticular conditions, or for electric insulation, there are required high molecular weight fluorinated compounds which (i) are liquid over a wide range of temperatures, (2) have a relatively low vapor pressure and (3) exhibit a high degree of chemical and thermal stability. For these and other applications, perfluorinated products are highly suitable, i.e., products which do not contain appreciable amounts of elements other than carbon and fluorine and, in particular, do not contain hydrogen in their molecule. Such perfluorinated products, in fact, generally possess the highest characteristics of chemical inertia and often of thermal stability.

2. Description of the Prior Art it is known that fluorinated and perfluorinated products having a rather high molecular weight can be readily obtained by polymerization and copolymerization of fluoroand perfluoro-olefins. Usually, however, the products thus obtained are high polymers having the appearance and characteristics of solid substances, either at room temperature or at somewhat higher temperatures. Accordingly, they are unsuitable for most of the applications referred to above, wherein it is necessary to employ materials having a low volatility but being liquid at room temperature and over a wide range of temperatures,

Attempts have been made to obtain high molecular weight fluorine-containing products possessing these characteristics by telomerization reactions of fluorowhich as a practical matter are the only telomers that can easily be obtained, exhibit a significant drawback whichhinders their use for many of the desired applications. Thus, the molecules of the telomers consist essentially of a regular sequence of equal (A) units bound oneto another by carbon to carbon bonds. This imparts to the molecules a considerable rigidityand a high tendency to crystallize. It, is also known that rotation around the C--C bonds is hindered by astrong energy barrier, .in. contrast to the condition existing with the C0 bonds. Thus, C-O bonds have a considerable freedom of rotation. It is also known that the linearity and regularity of structure of themacromolecules appreciably promotes the crystallization process. Consequently, when a telomer of, for example, a fluoroethylene has a value it sufficiently high to render its vapor pressure negligible or very low, it is normally a solid or a wax at room temperature. When the telomer is brought to the molten state by heating, it generally becomes a highly volatileliquid, having a low viscosity and a high variation of viscosity with temperature, so that it is accordingly, unsuitable for most of the desired applications.

It is known, for example from Belgian Patent 616,756,French Patents 1,359,426 and "1,362,548, to prepare perfluoroethers bypolymerizingepoxides of perfluoroolefins in the presence of active carbon or alkaline catalysts. The products thus obtained are polyperfluoroalkylenethers having a thoroughly regular structure as regards both the units forming the chain and their distribution and are characterized by the fact that each of their two terminal groups is the same in all chains. Theseproducts consist of chains whereinC-O and C-C bonds are regularly alternated '(.-C-C

O.C- -CO). As saiclbefore, CC bonds have a marked energy barrier which tends to oppose their rotation where-as this is not the case for C-O bonds.

It is desirable, moreover, to have available products having a higher incidence of- C--O bonds in'respect to C-C bonds in the polymeric chains. Furthermore, it is desirable to have available products containing peroxidic groups.

SUMMARY OF THE INVENTION wherein: C513,, is a perfluoroalkylene zero and 2, and preferably between zero and l, the

reaction conditions, and they consist of chains; wherein there can be present'sequences of C bonds and also -.OO'- bonds, and different terminal groups. Said products are obtained according to the present inven-' tion by means of direct reaction of p'erfluoropropylene with molecular oxygen or with a gas containing oxygen,

iniwhichR may be F or CF and 2) linear perfluorinat'ed polyethers and mixtures thereof of the general formula v oFs0- CiF.'-o 1. oFr-o oF-0)n(0)s-A unit derived from the opening of the double I bond of a hexafluoropropylene molecule, the different perfluoroalkylene units-having a random distribution along the polyether chain; A is a functional group selected from the group consisting of COF, CF COF and- CF(CF -,)-COF; and P, Q, R and S may be the same or different numbers, Q, R and S may each or all be equal to zero, the sum of P+Q+R being a number between I and 100, the ratio (Q+R)/P being a number between ratio S/(P+Q+R) varying between zero and 0.5 the ratio S/P being. a number between zero and 1,

preferably between zero and 0.5. When integer S is 7 zero, the linear perfluorinated polyethers (II) of this in- 'vention, for sufficiently highvalues of P, will exhibit the structure of true homopolyethers when Q and R'jin the above formula are zero, and are to be regarded as true copolymeric polyethers or copolyethers when perfluoroalkylene units different from C F are also present in. the chain, i.e. when 0 orR or both of them are different from zero.

It is noted that linear perfluorinatedpolyethers conforming to the foregoing formula (II) may possibly contain therewithin units of C F bonded directly to one another. Any such units are present in extremely minor amounts, i.e., less than about two per cent by weight, and if present do not affect the properties of the polyethers.

I DESCRIPTION OF THE PREFERRED EMBODIMENTS units. On the other hand, thefunits indicated by the symbol (-0-) correspond to the presence of peroxidic bonds. That is, these units do not form-sequences and must be understood as always being between two fluoroalk'ylenoxy units. I

p The polyetherstll) of this invention are usually obtained in the formof a mixture of molecules having different molecular weights, different distributions of the various units, and presumably also different composi- 0 'tions. One can, of course, isolate from these mixtures pure chemical compounds, characterized by a given structure of the terminal group A, by a givendistribution of the various units in the chains, and by a precise value for the indexes P,Q,R,S, the last three indexes h'aving'effectivelyavalue of zero or of=a whole number.

It is, however, frequently preferably, in order to characterize the structure of the .whole polymer, to havev recourse .to concepts usuallyused in the field of the macromolecular chemistry and, more particularly in the field of copolymers andterpolymers, such as the concepts of average molecular weight and of average composition. In this case, the formula II reported above remains perfectly valid, buteaeh of indexes P,Q,R,S represent an average value and can therefore have a value not necessarily corresponding to that of a whole number. Moreover, the structure of terminal group. A

cannot in this case be indicated by a simple formula since it results from the contribution of the aforementioned possible different structures- I I The'present invention also relates to a process for th preparation of perfluoropropylene epoxide, COF

units of one or both of --CF -O and CF(C,F .O- units, such homopolymers or copolymers containing from zero to 5 peroxidic oxygen atoms per 10 combinedoxy gen atoms and having as the terminal groups the group. CF O- at one end and at the other end vthe functional group COF, CF COF or CF (CF3')COF The process comprises subjecting perdiluted with an inert'solvent, to a photochemical reaction with molecular oxygen at a temperature between about l00C and'+80C, at a pressure between about 0.1 and 40 atmospheres, in the presence of ultraviolet radiation containing at least 1 percent of radiation having a wave length less than 3,300 A, the oxygen being fed to the liquid reaction phase in such amount as to maintain the liquid phase continuously saturated with oxygen.

In order to maintain perfluoropropylene in the liquid phase at the temperature selected for the reaction, a sufficiently high total pressure (which can be as much as'40 atmospheres) is used. As canbe seen from the experimental examples reported hereinafter, in the range.

' the chemical structure of the reaction product. However, the pressure must be such as. to maintain in the liquid phase at least most (i.e., greater than 50 per cent and preferably greater than .per cent) of per- ,fluoropropylene present in the reaction zone and the partial pressure of'molecular oxygen must be of at least 0.1 atmosphere.

The process may be conveniently carried out by passing a stream of molecular oxygen or of an oxygencontaining gas such as, e.g., air, through a liquid phase of hexafluoropropylene, in the presence of U.V. radiations as previously defined. Within the scope of our process, one can select operating conditions whereby there is obtained a high degree of specificity towards the formation of one type of products rather than of another among the products previously defined. For example, a high specificity toward the formation of the epoxide of C F can be obtained, i.e. a ratio between the epoxide and the higher molecular weight compounds of about 1:1 (50 percent epoxide) or more, when the process is carried out under pressure, preferably in excess of atmospheric, and at a temperature close to the boiling point of the liquid phase under such pressure. Conversely, the ratio between the epoxide and other reaction products having higher molecular weight decreases, and can be less than 0.01:1 as the operating temperature of the process is decreased, thus increasing the difference between the temperature employed and the boiling temperature of the system under the adopted pressure.

The structure of the linear polymeric products and mixtures thereof included in the general formula II are highly influenced by two main parameters of the reaction: l the temperature and (2) the irradiationintensity of the liquid reaction phase. By appropriate selection of the operating conditions for these two parameters it is therefore possible to direct the reaction toward the formation of one type of product rather than toward another.

It has been found that essentially polymeric products are obtained of the formula wherein P, S and A are as previously defined, by carrying out the reaction at temperatures lower than about -l0C, and preferably between about -80 and 40C.

Indeed, in the lowest range of temperature the content of perfluoroalkylenoxy units other than -C F O in the molecular chain of the resulting polyethers is so low as to have virtually no appreciable influence on the properties of the products and these products may be considered to be of the homopolyether type.

When the reaction is carried out at a temperature of about -lOC there are present in the mixture of final polyethers minor amounts (about 2-3 percent by mols) of other perfluoroalkyleneoxide units different from the principal unit -C F O. When operating at higher temperatures, and particularly at temperatures higher than 0C, the percentages of units of CF O and/or in the reaction product increases. Thus, the higher the temperature, the higher the percentages of such other units, so that these units become a very important characterizing feature of the copolyether chain. Thus, by operating at increasingly higher temperatures and approaching the limit of about 80C, the copolyether Thus, when a temperature above 10C is used, the average molar ratio between the units -CF '--O- and and the units C F O, will have a value within the limits of 0.02 and 2. This ratio, as will also be seen in the following experimental examples, increases upon increasing the reaction temperature.

In addition, the temperature influences very markedly the average molecular weight of the polymeric products, i.e. the value of the sum of P+Q+R. The highest average molecular weights will generally be obtained at the lower temperatures whereas lower average molecular weights are obtained by operating at higher temperatures.

Moreover, it is also possible to regulate the average molecular weight in order to obtain the desired value by varying the concentration of C F in the liquid phase. The higher molecular weights are obtainable by using a high concentration of C F e.g., by using undiluted C F whereas lower'molecular weights are obtained by diluting the C F with a solvent.

As previously pointed out, the crude polymeric product obtainable by the process of this invention is generally characterized by a rather wide distribution of molecular weights, as usually occurs in all telomerization, oligomerization and polymerization reactions. it is therefore necessary to have recourse to average values of molecular weight in order to characterize the entire crude polymeric product.

Another important characterizing feature of our polymeric products is the content of peroxidic oxygen, for example, which is shown by one of the ratios S/P, S/(P+Q+R) or S/(P+Q+R+l). This last ratio is the most meaningful insofar as it represents the ratio between the number of peroxydic bridges and the sum of all the C-OC- and -CO--OC bridges present throughout the chain.

As previously noted, the content of peroxydic bridges in the crude polymeric product is such that the SIP ratio can vary from zero to l.

The concentration of peroxidic groups depends on the intensity of irradiation and can be varied within the limits desired by utilizing suitable average irradiation conditions in the reaction zone. The concentration of the peroxidic groups depends also on the degree of conversion actually obtained during the reaction.

The average intensity of irradiation of a reaction system is in general a quantity that is difficult to define by numbers, since it depends on several parameters and is highly influenced by the particular geometry of the reaction system. A meaningful indication of the average value of the irradiation intensity in a sufficiently symmetric reaction system can however, be inferred from a consideration of three fundamental elements:

l. the amount of useful U.V. radiations having a I wave length lower than 3,300 A penetrating the reacting phase, E (watts);

2. the surface through which the radiations penetrate the reaction system, S (cm and 3. the volume of the reaction system, V (cm).

If we consider, e.g., the particular instance in which the U.V. radiation source is placed completely inside the reaction system and the surface S consists of a material that is completely transparent to the useful U.V. radiations, the value of E can be considered as equal tothe amount of radiations, having useful-wave length, emitted by the source. If on the contrary, either because the U.V. source is placed outsidethe reaction system or because between the U.V. source and the reacting system there is placed'a medium having a certain absorption power for the radiations, so that only a portion of the useful radiations emitted by the source reach surface S or in any event penetrate the reaction system, the value of E can then be calculated, either through a simple consideration of geometric factors or by a real, measurement of the quantity of useful radiations as can be obtained by having recourse to actinometric methods, well known to people skilled in the art.

The value of surface S must be considered in an appropriate manner, namely, by referring to geometric surface of an ideal type which most nearly could be compared with the actual surface.

In other words, the value of S must be calculated without taking into account surface irregularities or slight differences'with respect to the perfect geometrical form. The reaction volume must be considered as equal to that which can be actually reached by the U.V. radiations, without taking into account the possible phenomena of absorption of the radiations by the liquid medium.

We have observed that, in order to represent in a meaningful waythe situation of average irradiation which characterizes a particular reaction system and which would directly influence the formation of relatively more or less peroxidized reaction products, one may have reference to an averageirradiation index l, which is defined by the equation wherein E,'S and V have the aforedescribed meaning.

We have ascertained that it is possible to obtain, from liquid perfluoropropylene and oxygen, reaction products having a desired content of peroxidic groups, by using an average irradiation index of from 0.1 to 50 watts/cm? A low content of peroxidic oxygen, i.e. S/(P+Q+R+l)-less than 0.2, is obtained by adopting reaction conditions whereby index I is greater than 2 and preferably greater than 3. On the contrary, with values of l less than 2, or preferably less than 1, polyethers containing substantial content of peroxidic groups, i.e. S/(P+Q+R+l) greater than 0.2 can be obtained.

It should be noted, however, that not only the irradiation conditions will influence the extent of the peroxidic nature of the reaction products. Thus, other reaction conditions, such as, e.g., the degree ofconversion, will also affect this characteristic of the products. More particularly, it has been ascertained that even in the presence of a sufficiently high average-irradiation intensity (I. greater than 2), the polyether products formed in the initial step of the photochemical reaction between liquid perfluoropropylene and oxygen, may contain a considerably quantity of peroxidic groups. The average content of peroxidic oxygen of the products decreases rapidly, however, as the reaction lar value of l. Conversely, even by using a rather low intensity of irradiation, for example, lower than 1, it is possible to obtain polyethers having a reduced content of peroxidic oxygen, such as S/(P+Q+R+l) lower than 0.2, by carrying out the reaction to a high final degree of conversion, for example, of the order of 60-70 percent.

The statements previously made relating to the effect of the average-irradiation intensity on the peroxidic character of the reaction products should, in a strict sense, actually be referred to theproducts obtained at.

conversions not less than about 5 percentand not greater than about percent.

I Additionally, it hasv been ascertained that the reaction temperature exerts a certain influence on the characteristics of the products, in the sense that by lowering the reaction temperature belowabout 65C the irradiation conditions being the same, the reaction products tend to have a higher content of peroxidic groups.

As regards the amount of oxygen to be employed in order to maintain the liquid reaction phase saturated with oxygen, it was ascertained that an excess of oxygen should be used with respect to the amount of oxygen consumed during the reaction. In other words, the rate of oxygen fed into the reaction zone should exceed the rate at which the oxygen is being consumed during the reaction.

'. For example, when operating atabout atmospheric pressure, the excess of oxygen in the liquid reaction phase can be obtained by bubbling into the reaction mixture an amount of oxygen, either in pure state or diluted in an inert gas, that is at least twice that amount that is simultaneously being consumed. The excess of oxygen leaving the reactor carries along such volatile reaction products as COF andCF COF. It is also possible to operate without having an outflow of oxygen from the reactor. In such instance, in order, to operate in the presence of an excess of oxygen, it is necessary to maintain a high oxygen'partial pressure in the reactor while the reaction is carried out. This can be obtained, for example, by operating at low temperatures (of the order of -40 to 60C) and at a pressure higher than atmospheric, preferably above 4 to 5 atmospheres and by continuously maintaining such pressure so as to replenish the amount of oxygen consumed. In thisinstance, the high pressure maintains the partial pressure of the volatile reaction products in the vapor phase at a low value, soas not to disturb the reaction that thus can continue so long as there is oxygen available in the liquid mixture, i.e., the oxygen concentration in the liquid mixture is maintained at saturation.

We have also found that it may be convenient to carry out the photochemical reaction between oxygen and perfluoropropylene in the presence of a liquid phase by adding to the reaction system another compound which is liquid under the reaction conditions. This diluent maybe any of various compounds which do not appreciably react with oxygen under the selected irradiation conditions. The diluent may or may perfluorocyclobutane,

not act as a solvent for either the perfluoropropylene used in the reaction or for some or all of the reaction products.-

Compounds which are suitable for this purpose include, for example, perfluoro compounds such as perfluorodimethylcyclobutane, liquid perfluoro-paraffins,

' perfluorobenzene, perfluoroamines such as tri-perfluorobutylamine, straight chain or cyclic perfluoro ethers such as for example perfluoropropylpyrane, and oxygenated perfluoro compounds which may be obtained according to the present process, such as hexafluoropropylene epoxide. In addition, wholly or partially chlorinated compounds maybe used as the reaction medium, e.g., carbon tetrachloride, chloroform, methylene chloride, methylchloroform, or chlorofluoro derivatives of methane, ethane or propane, such as CF Cl, CF Cl CFC1 Cl-lF Cl, CHFCI CF ClCF Cl, CFCL CF C1, CC1 CF CLC1-1 ,CF CFC1CF C1 etc.

The reaction may be carried out according to an essentially batchwise, technique. In such case,.into a reactor containing the initial charge of liquid perfluoropropylene either in the pure state or in solution in preferably per-halogenated solvents, at the pressure and temperature conditions selected for the reaction, with irradiation by means of an UV. light from a suitable source such as a mercury vapor lamp, there is introduced a stream of molecular oxygen or of a gas containing molecular oxygen such as air, such introduction preferably being across the entire liquid phase. The excess oxygen leaving the liquid phase is saturated with perfluoropropylene and also contains most of the'low molecular weight degradation products and other volative reaction products such as, e.g., the epoxide C F O. By means of a suitable reflux condenser, most of the entrained perfluoropropylene is removed and recycled back to the reaction zone, while the low molecular weight products having an acidic character are separated from the, oxygen by washing with water or alkaline solutions.

The thus purified oxygen, after careful drying, may be recycled to the reaction, together with added oxygen to replace the amount already consumed in the reaction. The reaction is carried on under the foregoing conditions until the conversion of the desired amount of initial perfluoropropylene is reached. Thereafter the UV. irradiation is stopped and by distillation of residual perfluoropropylene, if present, and of cyclic ously removed from the system. By suitable means, e.g., by distillation perfluoropropylene is separated from the reaction products in such portion and is continuously recycled to the reactor while the amount of perfluoropropylene consumed by the reaction is taken into account and added as make up.

The determination of the actual average structureof the linear polyethers may be carried out by suitable chemical or spectroscopic analysis.

tions, have terminal chain groups generally consisting of CF O- groups and of COF groups, these last groups being bound either to'an oxygen atom or to a carbon atom, such as, e.g., CF,COF, or

CFCOF These COF groups are revealed in the infrared absorption spectrum by a characteristic absorption in the 5.25 zone. nuclear magnetic resonance spectrum of F gives all the other desired data, both qualitative and quantitative, to identify the nature of the units in which fluorine appears and their respective amounts.

In this spectrum, the presence in the chain of the group OCF -CF(CF )O is indicated by the resonance of 5 fluorine atoms in the zone of p.p.m.

(from CFCl and of 1 fluorine atom in the zone of +144 p.p.m. The resonance'bands in the zones of +49 p.p.m. and +51 p.p.m. are due'to the two fluorine atoms of the group OCF O- whereas the bands in the zone of +55 p.p.m. show the presence in the chain of repeating units (OCF with n 2 2. The resonance in the zone of p.p.m. indicates the presence of the tertiary fluorine atom in the --O CF(CF )O group.

In the same .N.M.R. spectrum there are also indicated, as shown in the following tab1e,,the different terminal groups that may be present inlthereaction products obtained from the photochemical reaction.

The presence of peroxidic oxygen in the product is indicated and its content determined by reacting a sample of the obtained product with Nal dissolved in acetic anhydride and then titrating the freed iodine with thiosulphate. Thus, 200 mg of product are dissolved in 5 cc of CF Cl-CFCI To this solution are added 20 cc of acetic anhydride and 2 g of Nal. The whole is stirred for 1 hour at room temperature; then 200 cc of water containing 2 g of K1 are added thereto, followed by ad-' ditional stirringwfor a few minutes and then titrating with 0.1 N sodium thiosulphate. The grams of active oxygen pen 100 grams of' product are calculated using the-formula (8 j n) lOQ p) grams of active oxygen/100 g product wherein n indicates the cc of 0.1 N solution of thi osulphate used and p is the amount in grams of the weighed product.

The: presence of ,peroxidic groups is also clearly indicated by the Nj.M.R. spectrum of fluorine, since it shows'resonance bands in the zones of 75, 85, 89, -l34,

137 and 1.42 ppm. from CFCl The; presence of units of C l bonded directly 'to each other is considered to be indicated by the'N.M.R. spectrum of fluorine, since it shows resonance bands in 'the zones between +68 and +73 ppm. from CFCl used as is forvarious applications, and fractions,

characterized by a relatively restricted molecular weight distribution, such as those obtainable by simple distillation, may be entirely suitable, without the necessity of isolation ,as pure chemical compounds. However, pure compounds'that are homologous members of the series of products within the scope of the general formula of the; products of this invention can. be separated from :the crude mixture. An example of the a series having the formula 1 CF; O (C F O) A is the compound and its higher members as shown in Example 10 hereinafter.

Furthermore, pure products belonging to series that can be represented by the formulas were separated and characterized as shownin Example Cyclic ethers obtained according to our process are: C F O perfluoro-4-methyl-l ,3-dioxolane (b.p. 8C)

and cm o perfluoro.-2,4-dimethyl -l,3-dioxolane (b.p. 325C) I CFa-CF CF: s t) A; c (5F; v.

These two cyclic ethers are newchemical products characterized by extremely high chemical and thermal resistances,

The fieldsof applications of the products of the invention are remarkably wide 'due' to: the particular chemical structure of the products considered.

For instance, thoseproducts containing' a high con tent ofperoxidic groupsfind utility as' cross-linking agents for elastomeric polymers such as'fluorinated polymers and copolymers, e.g. copolymers of vinylidene fluoride and hexafluoropropylene.

- T he non-peroxidic*polyethers are liquids which, depending upon their molecular weights, may have a boiling temperature from as lowas of the order of l0 -20 C, under normal pressure v(low molecular; weight materials) to more than 200C under, reduced pressure of -1 mm Hg (high molecular weight materials). They have very high chemical and thermal stability and exhibit very goodylubricating properties. For these reasons theyvma'y be used as hydraulicfluids, heat exchange liquids,a nd/or as lubricants under particularly severe temperature conditions.

, For'certain applications, such as those involving use at very low temperatures (down to l00C)"and those wherein onlya very low variation in the viscosity'atdifferent temperatures is permitted, the copolymeric polyethers are preferred over the homopolymeric polyethers, since the former show a higher incidence of C.O bonds in the oligomeric chain. This leads to a lower rigidity'in the molecular structure, with theadvantage that the products exhibita' lower viscosity at a given molecular weight, or a lower volatility at agiven viscosity.

Another advantage is afforded by virtue of the low variation in viscosity with temperature. It is well known in fact that, whereas C-C bonds have a marked energy barrier which tends to oppose their rotation, this is not the case for C--O bonds, and therefore a higher ratio --C-O/CC- bonds in the main chain causes the above described effects. Homopolyethers'are thus preferably used for those applicationswherein an extreme chemical and thermal stability is required, such as applications for heat-transfer and lubrication under conditions of high temperatures, high pressures and/or in the presence of strongly reactive chemicals.

The cyclic ethers can be used as solvents or plasticizers for halogenated organic compounds, generally, and in particular, for fluorinated organic compounds.

The following examples will further illustrate our invention. All parts are by weight unless otherwise stated.

EXAMPLE 1 An apparatus was set up consisting of a three-neck glass flask having a capacity of- 1.5 liter and provided with a thermometer, a gas inlet dipping tube reaching the bottom and communicating with the atmosphere through a reflux condenser cooled by a cooling mixture maintained at 7 8C.

lnto the reactor there was introduced a quartz ultraviolet-ray lamp of the Original Hanau- Q 81 type, having a tubular shape and a size of 245 X 20 mm. This lamp had an absorption of 70 watts and generated a wave-length emission mainly between 2,400 and 4,400 A, amounting to" 12.8 watts. In such emission the radiations having a wave-length lower than 3,300 A corresponded to 3.8 watts. The calculated index 1 was between 3.5 and 4. 1230 g of pure perfluoropropylene were condensed into the reactor, which was maintained by external cooling means at a temperature of 78C.

While maintaining the external cooling so as to keep the temperature of the liquid between 60 and 30C, the UV. lampwas switched on. By means of a circulation.pump, a stream of anhydrous oxygen (130 1/h) was sent through the inlet pipe dipping down to the bottom of the reaction .vessel. The gas leaving the reaction vessel after having passed through the reflux condenser was washed with an aqueous KOH solution having a concentration of 20 percent and then collected in a 50 liter gasometer from which, after drying, the gas was once more picked up by the pump and recycled into the reaction zone. Oxygen in an amount equivalent to that consumed in the reaction was periodically fed to the gasometer.

After 28 hours, about 75 N1 (liters under normal conditions) of oxygen were-absorbed and the reaction was stopped. The unreacted perfluoropropylene and those reaction products having a boiling temperature below 30C at atmospheric pressure were separately distilled and removed from the reaction vessel. 650 g of a mixture containing 78 percent by weight of Cal and 19 percent by weight perfluoropropylene epoxide (b.p.

wherein A is COF with a ratio of the two fluoroformate the (Q+R)/P ratio was about of 0.03 and the R/Q ratio was about of 0.1. The N.M.R. spectrum did not show resonance bands due to peroxidic groups. By iodometric analysis carried out as previously described, the presence of active oxygen was determined in an The products were distilled without reflux. The following fractions were thus obtained.

Fraction Distillation lnterval Grams a) 3040C/760 mm 11 b) 40-64C/76O mm 8.5

50C/20 mm C/20 mm 37 d) 5SC/0.5 mm 100C/0.2 mm 40 e) 100C/0.2 mm C/0.2 mm 53 f) 155C,0.2 mm 350C/0.1 mm 462 g) residue 30 Fractions a), b) and c), which were liquid, had sharp, acrid odors and developed hydrofluoric acid fumes when exposed to moist air. They were miscible in ethyl ether.

Fractions d) and e) were put together and the mixture was subjected to careful fractionation in a rectifying column while operating under a residual pressure of 10 mmHg. In this way, the fractions reported hereinafter in Table l were separated. In this table there are also reported data relating to density, viscosity, equivalent acidimetric weight, and percentage composition determined on various fractions.

The infrared absorption spectra of the various fractions all were similar one to another, presenting absorption bands in the 5.25 p. zone and in the 5.6 ,1 zone, due

to the presence of COF and COOl-l, groups, respectively. The intensity of these absorption bands decreased for the various fractions as the boiling temperature increased.

Other infrared absorption bands present in all the fractions occured in the zones between 7.5 and 9.2-;1 and also at 10.15, 11.2, 11.5, 12.05, l2.35,and 13.4 t.

Solubility tests of the various fractions in ethyl ether showed that, while fractions 1 and 2 could be mixed in all ratios with the ethyl ether, fractions 10 and 11, on the contrary, were practically immiscible therewith. The other fractions showed an intermediate behavior.

All of these fractions were completely miscible in all the perfluorinated solvents examined.

Fraction f) had an average density d of 1.8953 and an average equivalent acidimetric weight, of about 4,000, as determined in an aqueous NaOH solution in accordance with the conditions described in Table 1. The average percent composition was C 21.6- percent; F 68.5 percent; 0 9.9 percent.

In fraction f) the following viscosities were determined at various temperatures:

The infrared absorption spectrum of the product of which fraction f) consisted revealed, besides the presence of small absorptions in the zones of the COF and COOl-l groups, a wide absorption between 7.5 and 9.2 p. with a maximum of about 8.0 p. and

other characteristic absorptions at 10.15, 1 1.2, l 1.5, 12.05, 12.35,and 13.4 t.

50 g of fraction f) were heated with 5 g of KOl-l in the form of pellets for a period of 2 hours at a temperature of. 240-250C at. atmospheric pressure, in a l00-cc flask which was part of a distillation apparatus. During this treatment, the development of carbon dioxide, fluoroform, and water vapor were observed. At the end of thistreatment, the contents of the vessel were subjected to vacuum distillation. About 40 g of colorless, transparent oil havinga boiling range between 120 and 200C at 0.2 mm Hg'were thus obtained. This product no longer showed an acid character, was completely non-reactive towards water and alkaline solutions, and had an infrared absorption spectrum in which the absorptions due to the acid functions were. completely absent.

Average molecular weight was determined to be of the order of 3,000.

By'N.M.R. analysis the chain was shown to consist essentially of the same structure as the starting product, except that the terminal group A (fluoroforrnate isomer groups) had become a mixture of CF H and --CFl-l'---CF in a ratio of about 3:1. The terminal group -OCF H- was-revealed by the resonance bands of 2 atoms of fluorine at +833 ppm. from CFCl The terminal group -OCFH-CF was revealed by the resonance bands of '3 fluorine atoms at +85 p.p.m. and of 1 atom of fluorine.at+146.2 p.p.m.

The residual fraction g) had a viscosity at 24C higher than 2,000 centipoises, a density d of 1.9104, and showed an exceptional resistance to thermal treat-- ment, both in air and under high vacuum, without indicating any symptom of modification in structure after prolonged periodsof heating at temperatures of about 400C. The average percent composition was C 21.5 percent; F 68.7 percent; 0 9.8 percent. The infrared absorption spectrum of this fraction was completely similar to that of thepreceding fractions, except for the veryv low intensity of the absorptions'corresponding to the acid groups. I

Fractions f) and g) were miscible in all proportions with all the perfluorinated solvents examined, such as,

tylamine, and perfluoropropylpyrane. They were, by contrast, immiscible with conventional organic solvents, such as, for example, acetone, ethyl ether, tetrahydrofurane, toluene, CCl CHCI CH Cl dioxfor example, perfluorocyclobutane, perfluorotribu- 0.4 liter, in which the U.V.-ray lamp was contained, was used as the reactor. 165 g of perfluoropropylene and 200 cc of pertluorocyclobutanewere collected in the reaction vessel by distillation at --78"C. The reaction was started by passing into the reactor an oxygen stream (about 1/h) and lighting the U.V.-lamp, with thetemperature at -45C. The reaction was continued for a period of 11 hours, during which time the temperature of the liquid phase gradually rose until' it 10 reached--9C and a total of about 18 N liters of oxygen were absorbed. Under these conditionsthe value of the index 1 was greater than 5. v i C F the unreacted perfluoropropylene, and those products having a boiling temperaturelower than 25C 3 at atmospheric pressure were distilled off. The residue consisted of g of a liquid product having the average percent composition andthe average molecular weight corresponding to (C F O wherein n is about 14-16. The N.M.R. spectroscopic analysis indicated that the product had an average formula cF;-0 (O3F O)r-(GF:0)q(OF-0)n(0-)s wherein the (Q+R)/P ratio was about 0.05, the R/Q ratio was about 0.1, and A was essentially the COF group.

Iodometric analysis showed the presence of active oxygen in amounts corresponding to a ratio S/(P+Q+ R+l of 0.03.

The product gave the following fractions when sub jected to distillation 1 45 presence of a solvent during the reaction resulted in the formation of a product having a lower average boiling ane, dimethylsulfoxide, dlmethylformamide, ethyl rat re acetate, etc. empe u TABLE 1 Distillation Viscosity Percentage interv' Equivalent (centicomposition Number 01 0.) at 10 acidimetric poises fractions g. mm. Hg (124 weight at 24 C C F The equivalent weights reported were obtained by introducing about 0.4 g. of exactly I weighed product into 25 cc. of 0.1 N NaOH keeping the whole in strong agitation for 2 hours ions was considered as the equivalent acidimetrie weight.

EXAMlLE 2 i The same apparatus as in Example 1 was used, except that a cylindrical glass vessel having a volume of EXAMPLE 3 Under the conditions of the preceding example, 135 g of C F and 340 g of CCl., were reacted with oxygen.

After 6 hours of radiationwith continuous bubbling of oxygen (50 l/h) at temperatures comprised between 3 7 and C, 7.5 liters of oxygen had been absorbed.

The reaction was stopped and, after removal by distillation of the products which were volatile at room temperature, two liquid layers resulted. The lower liquid phase (about g) was separated and gave fractions of products having boiling temperatures between 40C/7 60 mm and 230C/ /0.3 mm when distilled. The upper liquid layer gave, after removal of CCl.,, 8 g of liquid products containing only C, F and O and having-boiling temperatures between 80 and 210C/760 mm. At the same boiling temperature, the products obtained showed characteristics completely equivalent to those of the products described in Examples 1 and 2.

EXAMPLE 4 EXAMPLE 5 An apparatus was assembled consisting of a cylindrical glass vessel having a capacity of 0.4 liter and provided with a thermometer and a gas inlet tube dipping down to the bottom and communicating with the atmospheregby means of a reflux condenser cooled at 78C and containing an ultraviolet-ray lamp of the type defined in Example 1. In this vessel, 460 g of C F were distilled at 7 8C and the photochemical reaction was started by radiation with ultraviolet light and by feeding a stream of dry air (60 l/h) to the liquid phase kept at 70C. The air left the reactor and was removed after passage through the condenser at 78 C, which recycled at least a portion of the entrained C l back to the reactor. As the reaction proceeded, the temperature of the liquid phase rose gradually until it reached 25C,'after about 8 hours of reaction. The liquid product remaining in the reactor (108 g) was distilled and separated into the following fractions:

A) 5 g -57C/760 mm B) ll g 4598C/18 mm C) g 80-l66C/0.3 mm D) 90 g l66260C/0.3 mm E) 25 g residue These had characteristics completely equivalent to those of the corresponding products described in Example 1.

EXAMPLE 6 containing a high percentage of radiations having a wave-length lower than 2.600 A and an absorption of 8 watts. In this lamp those radiations having a wavelength lower than 3,300 A corresponded to 0.9 watts by working at room temperature. This source of U.V. light was contained in a tubular quartz sheath having a size of 245 X 20 mm and was immersed into 490 g of liquid perfluoropropylene placed in a 0.6 liter glass vessel provided with a dipping tube for the introduction of oxygen, and a reflux condenser kept at 78C, which vessel was immersed in an outer cooling bath. With this experimental apparatus the irradiation index I was calculated to be less than 1.

A closed system was prepared for. the circulation of molecular oxygen. By means of this system the oxygen withdrawn from a l0-liter gasometer by means of a circulating pump and dried, was fed to the reaction vessel and, when leaving the latter through the condenser at 78C, was washed with anaqueous KOH solution and recycled to the starting gasometer. The reaction was started by activating the U.V. lamp, keeping the perfluoropropylene at a temperature between 65 and C, and by feeding oxygen through it at a flow rate of about 50 liters/hour.

After ll hours, 2.4 liters of oxygen had been absorbed. At this point thereac'tion was stopped and the unreacted perfluoropropylene was removed from the reactor by distillation at 30C. It contained about 0.3 percent of epoxide.

l7.0 g of a liquid-semisolid product were obtained as the residue which analyzed as:

These data are very close to an average limit formula 3 6 2)fl- The N.M.R. spectrum showed that this substance consisted essentially of groups of CF(CF )CF that were bonded to each other by oxygen bridges prevailingly of the O-O (peroxidic) type and only in part by O-(ether)bridges. lt furthermore was shown by the N.M.R. spectrum that the terminal groups were essentially OCF and OCOF in 1:1 ratio and in such amounts as to lead to the formula (C F O L, with a value of 11 equal to about 40.

The presence of oxygen in the peroxidic form was also demonstrated by iodometric titration carried out as previously described. There resulted 7.8 g of active oxygen per grams of product, which corresponded to 0.9 atom of active oxygen per C F unit.

The polyperoxide of perfluoropropylene thus ob-' tained was remarkably stable at room temperature. When heated in the pure state to a temperature above 70-80C, it decomposed in a violent manner by evolving gaseous and low-boiling products, leaving practically no liquid residue.

EXAMPLE 7 Under the reaction conditions as described in Example 6, but operating at a temperature of 29C and with a molecular oxygen flow of 20 liters/hour, a photochemical oxidation of 505 g of perfluoropropylene was carried out for 22 hours. At the end of the reaction, by distillation of the unreacted olefin, there were obtained 71 g of a liquid acid product 19 having a high viscosity at room temperature and a percent composition corresponding to the formula (C F O 1.8)n- V I The N.M.R. analysis showed that the chain consisted prevailingly of C l units bonded by ether and peroxidic bridges in a ratio of about 1:1. There were also present inthe chain CF O units in a ratio to C F units of about 1:15.

The terminal groups present were mainly CF O CF CF(CF )-O-- groups with minor amounts of The iodometric analysis was in agreement with a content of 0.5 atom of active oxygen per'C F unit present in the chain.

This product showed an acidimetric equivalent weight'of 1000, as determined by prolonged agitation of a sample with a cold 0.1 N' NaOH solution and a back titration of the unreacted alkali excess andof the hydrolyzed fluoride ions of the COF groups.

This example shows'that, by varying certain conditions as compared to those described in Example 6 (more particularly, by increasing the irradiation time and the reaction temperature), it is possible to obtain products having an intermediate composition between that of a polyperoxide and that of a polyether of perfluoropropylene.

'EXAMPLES This example was carried out in the same manner as that described in Examples 6 and 7 with a U.V. lamp having an emission of 0.9 wattsin order to carry out a photooxidation of 700 grams of perfluoropropylene'at a starting temperature of 30C, using an oxygen feed flow rate of 20l/h.

The photooxidation was carried out-for a period of 560 hours while the temperature increased until a temperature of .lC was attained. At this point there were obtained, after evaporation of the unreacted monomer and of the volatile reaction products, 560 grams of a polymeric product having a percent composition corresponding to the formula (C F O and containing (by iodometric analysis) 0.08 atom of active oxygen per C F O unit.

This example shows that it is possible to obtain polyether products with a slight content of peroxidic bridges directly from the reaction, by increasing the irradiation time and consequently the conversion degree 81 Hanan type high-pressure mercury-vapor U.V. radiation generator was immersed. With these conditions the average irradiation index was about 4 watts/cm. A dipping tube to the bottom of the reactor permitted the introduction of an oxygen flow which then left the reactor, through a condenser kept at -7 8 C. .The unreacted oxygen was washed with alkaline solution and sent into a 50 liter gasometer from which,

by means of a circulating pump, it was continuously reintroduced, after ;drying, into the photochemical reactor. The amount of oxygen consumed in the reaction was periodically replenished in the system.

To the photochemical reactor, a perfluoropropylene flow was also continuously fed from a 50 -liter gasometer by means of a circulating pump.

The level of the liquid phase in the reactor was maintained constant by a continuous discharge, through the bottom, of a corresponding amount of liquid, which was sent to a continuous fractionated distillation system. From this system, the olefin and the compounds, if any, boiling, below 20C, were recycled as gases to the gasometer and the liquid reaction products. were collected separately. The reacted perfluoropropylene was. periodically replenished in the system. 7

With the described apparatus, a reaction was carried out by initiallyintroducing into the reactor, 600 g of C F and by feeding through it, at a temperature of to 30C, an oxygen flow of 80-100 liters/hour and a perfluoropropylene flow of about 100 liters/hour.

After 42 hours, 330 N liters of oxygen were adsorbed and 2,850 g of polymeric liquid products were obtained. Analysis of'the residual C F in the system showed that it contained 22.2 percent by weight of epoxide C F O, corresponding to a productionof 190 g of epoxide.

(which in this case was higher than 70 percent) even though adopting an irradiation index I lower than 1.

EXAMPLE 9 This example demonstrate that, although usinga relatively high irradiation intensity, it is possible to obtain polyether products characterized by a high content of peroxidic groups,,provided that the process is carried out so. as to maintain in the reaction zonea low conversion of C F for example lower than 20 percent. 'Itis desirable for this purpose to carry out the process ina' continuous manner, forexample as follows.

"An apparatus'was prepared which comprised a 0.5 liter glass reactorcoiitain'ing a liquid phase of perfluoropropylene, in which the previously described Q in 4:1 ratio. The neutral terminal groups of the chains 0-, and CF5-O-CF(CF )O groups in the respective ratios of 10:3:l,1whereas the terminal group of acidic nature consisted of --O-CF,CF(CF O-COF, OCF(CF )-CF 0COF, -0-CF ----O-. COF, and OCF COF in the respective ratios of 10:3.5:1:0.5.

As described hereinbelow, from the acid products obtained as. described above and having a certain content of peroxidic groups, by suitable treatments it is possible to obtain neutral products having a very high thermal and chemical stability. A treatment of this type may consist substantially of a neutralization with alkali and of thermal decomposition of the salts, thus eliminating the carboxylic. groups and most of the v p I 21 peroxidic bridges. 600 g of KOH (85 percent) in the form of pellets were introduced into a 3 liter vessel provided with an agitator, a reflux condenser and a charging tube. The vessel was heated to 100C and the slow introduction of the crude acid oil was started, while vigorously agitating. The temperature rose to l30-l40 "C while within 6 hours the introduction of 2.0 kg of fluorooxygenated product was completed. The salt formed was kept in agitation for a further 24 hours at a temperature of about 140C. By eliminating the circulation of water from the reflux condenser, the water contained in the vessel was'then permitted to distill together with a small fraction of neutral low boiling TABLE 2 Fractions Distillation g Composition Averagerange molecular weight w l 50-l00C/l mm Hg 460 C F O 600-1,000

ll lC/0.l mm 555 C F O 1,000-2,000

, 200C/0.1 mm e lll 20'0Cl0.l mm 300 c,r=,o, 2,500-3,500

350C/0.05 mm W residue 30 C F Q 5,000

All these fractions exhibited no oxidizing power and presentedan' exceptional chemical stability. In the infrared absorption spectrum of these products the presence of bands characteristic of acid groups could not be observed.

The spectroscopic analyses by N.M.R. showed that the structure of the chain was virtually the same as the structure of the chain of the startingproduct, however the structure of the terminal group A (fluoroformate isomer groups) had been changed'to a mixture of CF H and CFHCF in a ratio of about 3:1.

EXAMPLE The, photochemical reaction was carried out in a glass cylindrical reactor having a diameter of 245 mm and a volume of 22 liters, in the center of which there was placedcoaxially a Hg vapor lamp of the l-lanau No. 566] type, consisting of a tubular quartz well (sheath) having a diameter of 46 mm and a length of 250 mm containing an irradiating quartz element of the TO l200'type which emits a total of 34 watts of radiations having a wave length lower than 3,000 A.

In the reactor there were also placed a dipping tube reaching the bottom for the introduction of oxygen, a thermometric well (sheath) immersed in the liquid phase, a gas outlet tube, and another dipping tube for recycling C 1 The gas outlet tube was connected to a condenser kept at 78C by a mixture of alcohol and dry ice. The condensate wasrecycled to the reactor through the aforedescribed dipping tube while the residual gaseous mixture was passed to a washing system wherein it was bubbled first through water and then through a KOl-l aqueous solution. To the washed gas thus obtained there was added fresh 0;

coming from a gas reservoir (in order to replace that absorbed by the reaction)'and after careful drying over concentrated H SO ,the whole was passed back, by means of circulation pump, and bubbled into the reactor. The entire reaction system thus described was filled with oxygen and 25.75 kg of liquid C F (at its boiling point) were charged into the reactor. Thereafterfwhile circulating oxygen at a flow-rate of 1,000 l/h, the lamp was switched on.

After about 10 minutes the absorption of oxygen commenced with an initial rate (measured by a metering device inserted at the gas reservoir outlet) of about 250l/h.

The reaction was carried .out for 17 hours, during whichtime the. temperature of the liquid phase gradually rose from 30 to l0C and the absorption rate gradually decreased until it reached a minimum rate of l/h.A total of 2,280 liters of oxygen had been consumed (measured under room conditions). At this point the lamp was switched off and the reaction mixture was slowly heated up to 30C, while collecting and condensing the gaseous products distilling from the reactor. They weighed 6.60 kg and consisted of, unreacted perfluoropropylene (76.2 percent) and of the epoxide of perfluoropropylene (18.8 percent). The gaseous mixture also contained small amounts of products having a higher boiling point, which were found'to be analogous to those which the successive fraction consisted of.

The residual mixture remaining in the reactor was then heated to 100C, while bubbling oxygen through it in order to facilitate the removal of low boiling compounds, and was kept at this temperature for 3 hours, during which time there were distilled 640 g of a mixture of products essentially consisting of l30 g of hexafluoropropylene, 25 g of epoxide C F O, 30 g of perfluoro-4-methyll ,3-dioxolane (boiling point 8C), 1 10 g of perflu0ro-2,4-dimethyll ,3-dioxolane CFa-'(|1F(]J F,

o o P5 33 (boiling point 325C) 5 2 g of perfluorol methOxyisopropyl fluoroformate (boiling point 51C); 67 8 f perfluoro2-(5-methyl-4,7-dioxa)-octyl fluoroformate (boiling point l l.-l.l 4 at 755 mm, 85 at 270 mmHg) and the higher homologues, more specifically,75 g of boiling point .1558 at 755 mm, 82C at 35 mm), 25 g of (boiling point 935 at 20 mrnl-lg), and 20 g of I cri o-(omer-on ooF (extrapolated boiling point, 225-230C at 760 mm).

At boiling temperatures intermediate with respect to those of the aforedescribed oligomers, there were present minor amounts of oligomers of analogous structure but characterized by the presence of the following chain terminal groups (instead of CF;,O)

and

wherein it a 1 (boiling point 8s;90c),

wherein n 2 (boiling point 1 321389C), and wherein n 3 (boiling point 173180C), and products belonging to the series oF;-o cF-0 oF2-oF 0- ..-ooF

I CF:

wherein n -1 (boiling point 95-l05C), wherein n 2 (boiling point 144152C), and wherein n 3- (boiling point l85192C).

Higher oligomers which were not separated fro each other, by distillation were also present.

The residual oily product weighed 17.16 kg and had an oxidizing power corresponding to 0.37 active oxygen atoms per oxygen atoms contained in the oil and an experimental elemental composition of C3F O Various spectroscopic determinations and molecular weight determinations indicated that these products had the prevailing average formula CF O(C F O L042 C0F with a ratio of terminal groups to -CF -O-'-COl-" corresponding to about 5.

\ W' was calculated as higher than 3.

N.M.R. analysis showed however that the average ratio of CF O-- units to C F O units in the molecules was about 1:20. i

A sample -(l00 g).of' this product was subjected to distillation and the following fractions were obtained 5 g with a boiling point between 60 and C under atmospheric, pressure; 1 19.3 .g with a boiling point between 52 and 158C.at a pressure of 20 mml-Ig; 69.1 g with a boiling pointbetween 98 C (at 0.1 mml-lg) and 344C (0.7 mml-lg); and a residueof 1.6 gthat could only be distilled at higher temperatures.

The washing solutions (water and KOH) were mixed and analyzedyThey contained 24 mols of CO 72 mols of HF, and 24 mols of t-rifluoroacetic acid. I v

This examplethus illustrates that one may directly obtain reaction products with a 'very low content of peroxidic groups by reaction of C F with 0 upon using irradiation conditions such that the 1 value 100 X E)/(S V) is greater than 2. In this example this value was calculated as between 6 and 7.

EXAMPLE ll An U.V. lamp of the type described in Example 1 I was placed within'the quartz sheath; In the reactor air was replaced with oxygen- Then, by distillation, 1,050 g of perfluoropropylene were introduced and oxygen was passed through the dipping tube to a total pressure of 7 atmospheres, using for this. purpose a cylinder provided with pressure regulator. At this point the lamp was switched on while keeping the reaction-zone at 60C 4 by means of an outer bath of alcohol and dry ice. After a few minutes pressure in the reactor began to decrease. The pressure wasthen kept at thedesired value (7 atmospheres); by the introduction of oxygen from the cylinder, and this procedure was continued for 2 hours. At this point, the lamp was switchedoff, the pressure was slowly released, and the gaseous products were evaporated. These essentially consisted of unreacted perfluoropropylene, 0.6 g of the epoxide of perfluoropr'opylene and the oxidation products (COF +CF -COF)derived from 0.0275 mols of C F As the residue there remained 51 g of an oily product having an oxidizing power corresponding to 0.65 active oxygen atoms per 10 atoms of total oxygen contained,

and having an average elementalcomposition of (3 1 0 with an average molecular weight of about 3,200. In this example, the value of the! index (100 X El/(Sl Thus, this example shows that by adopting suff ciently high irradiation intensities, it is possible to operate under an oxygen pressure markedly higher than atmospheric pressure without obtaining appreciable formation of peroxidic products.

Moreover, since the operation was carried out at a in the chain. I

EXAMPLE 12 A system analogous to that described for Example The elemental composition of this product was C F ,OB1.32. r

In this example a filter (glass well) was used which, asshown by photometric measurements carried out separately, eliminated 90% of the radiations having a wave length lower than 3,300 A. Since the luminous power-penetrating the reaction system had thus been reduced to l/lO, the value of 1, which in the preceding example was about 3, in this example was reduced to 0.3. Thus, this example shows that at this low value of I r the oxidizing power of the product obtained was marwas employed for washing, drying and recycling of the temperature of the liquid was maintained at about 32- C and the U.V. lamp was switched on while contemporaneouslycirculating oxygen at a flow-rate of 100 l/h. After 1 hour and 35 minutes 10.7 liters of oxygen had been absorbed. The lamp was switched off and the gaseous and low-boiling products were distilled from the reactor.

The residual oily products amounted to 120 g, had an kedly raised.

EXAMPLE 14 An apparatus was employed which included a quartz test tube having a diameter of 18 mm and a volume of cc, provided with reflux condenser kept at -78C with alcohol and dry ice, and with adippingtube for the introduction of gas. In contact with a side of this small reactor and arranged so that the two axes were parallel, there was placed an I-Ig-vapor lamp of the low pressure Pen Ray type (without use of filters). This lamp has, in the useful zone, an emission of 05 watts.

38 g of perfluoropropylene were initially introduced into the quartz test tube, the lamp was switched on, and bubbling of an oxygen stream l0 l/h) was commenced. The irradiation was carried on for 5 hours.

The mixture was kept, during'thewhole reaction, at its boiling point. After having evaporated the volatile products at room temperature (essentially consisting of oxidizing power corresponding to 0.52 active oxygen atoms per l0'total oxygen atoms contained, and had an experimental elemental composition corresponding to (C3F5 Q5 OB&I.I8)HL I The average value ofn was between 10 and 20.

The gaseous and low-boiling products contained, in

addition to unreacted perfluoropropylene, 9 g of the epoxide of perfluoropropylene and minor amounts of the gaseous products described in Example 10. I

The washing solution was foundto contain 0.28 mols of HF, 0.09 mols of perfluoroacetic acid, and 0.09 mols I OfCO For this example the value of the 1 index (100 X E)/(S V') was calculated as about 3 in accordance with this value, the content of peroxidic groups for the total product was very low.

EXAMPLE 13 The apparatus described in Example 12 was used,

' but the quartz well containing the lamp was replaced by perature of the reaction mixture was kept at about 3 2 After having evaporated the volatile products at 1 room temperature (consisting mainly of unreacted C F along with 6 g of the epoxide of per-.- fluoropropylene), there remained as residue an oily product weighing 74 gand having a oxidizing power corresponding to 1.9 active oxygen atoms per 10 atoms of total oxygen contained. i

unreacted C 1 together with 0.1 g of the epoxide of perfluoropropylene), there remained as residue an oily product weighing 11 g and having an oxidizing power corresponding to 1.2 active oxygen atoms per 10 atoms of total oxygen contained.

The experimental elemental composition of this product was C F O Inthis example, the experimental set up made it possible to use only 1/6 of the useful U.V. light emitted by the lamp. Therefore the value ofl was calculated as about 0.75. Thus, this example demonstrates that also with this geometry of the system, a low value of I corresponds to a high content of peroxidic groups.

EXAMPLE 15 (COMPARATIVE) The same experimental arrangement was used as in the preceding example, but instead of the low-pressure lamp, there was employed a Pen Ray lamp provided with a suitable filter which eliminated all of the U.V. radiations except those at 3,660 A. The reactor, containing 40 g of perfluoropropylene, was then irradiated while bubbling in an oxygen stream (10 l/h) for 6 hours. After evaporation of the gaseous products, which essentially consisted of QR, no appreciable amount of oily product was observed. Thus, in this comparative example it was demonstrate that radiations having a wavelength of 3,660 A were essentially ineffective 'for the preparation of the polyether products of the invention.

' EXAMPLE 16 A photochemical oxidation was carried out using 35 kg of perfiuoropropylene kept in the liquid phase'at a temperature of 40 to -35C in a cylindrical reactor 27 (diameter 270 mm and a length of 250 mm) in the center of which a tubular quartz well was introduced having a diameterof46mm and containing an irradiating element of the Hanau TO 81 type which emits a total of 3.8 watts of radiations having a wave length lower than 3,300 A. To the bottom of the reactor was passed a stream of dry oxygen (100 l/h). The gases leaving the reactor, after passage through a reflux condenser cooled to-78C, were recycled (after adding make up oxygen to replace that amount consumed during the reaction, washing with alkali, and drying). The reaction was carried out for 110 hour, by which time 980 liters of oxygen had been consumed. By distillation of the unreacted perfluoropropylene and the volatile reaction products, 4.8 kg of polyether products were obtained in the form of a thick viscous liquid. They had an average elemental composition corresponding to the formula C F o and a peroxidic group content corresponding to 2.1 g of active oxygen per 100 g of product.

.The N.M.R. spectrum and the molecular weightdeterminations corresponded to a general formula in which P+Q+R about 3 2 (Q+R)IP 0.03 R/Q less than 0.1 S/(P+Q+R) 0.22

A was a COF group prevailingly present in the forms the ratio of these groups being 4:1. Thus, this example 1 shows that it is possible to obtain polyethers having a high content of peroxidic groups at a-degree of conversion not higher than 20 percent, with a low irradiation index I (in this case between 0.5 and 1), even when this is primarily due to the use of a high ratio between the reactor volume and the energy emitted by the UN. lamp.

EXAMPLE 17 1,070 g of perfluoropropylene were introduced into a stainless steel autoclave having an inner diameter of 70 mm and a volume of 800 cc, and provided with a coaxial inner well of transparent quartz having an outer diameter of 26 mm and a length of 185 mm, and with a liters/hour measured at atmospheric pressure, while.

through acontinuous feeding of gaseous oxygen, the pressure inside the reactor was kept constant at 7 atmospheres. An U.V. lamp of the high pressure Hanau TO 81 type wasintroduced into the quartz well; By

means of a bath placed outside the autoclave the tem-' perature of the liquid phase was adjusted at +1 0C, the lamp was switched on and, by appropriate regulation of the outer bath, the temperature was kept at +1 0C for 2 hours. With this irradiation arrangement, the index l was 4.4 watts/cm.

:zThe outlet stream was bubbled through an aqueous KOl-l solution in order to neutralize and thereby retain,

the volatile acid products formed in the reaction.

' At the end of the two hour period the lamp was switched off, the pressure was released, and the gases (unreacted C F together with the perfluoropropylene epoxide) were washed in the alkaline solution.

645 g of product containing 42 g of perfluoropropylene epoxide were thus collected. From the liquid product which remained in the reactor a fraction of 11 g, b oilingat between 0 and 50C, was separated by distillation. This fraction prevailingly consisted of perfluoro-4-methyl-1,3-dioxolane (b.p. 8C) and-perfluoro'-2,4-dimethyl-l,3-dioxolane (b.p. 325C). The residue consisted of 298 g of an oily polymeric substance which, by elemental analysis showed an average composition of 63.7% of F and 20.2% of C, corresponding to the formula cF O with an average molecular weight of about 1,200. By iodometric analysis (reaction with Nal in acetic anhydride plus CF,Cl-- CFCl, and successive titration with thiosulfate of the iodine released), there was determined acontent of 1.7 oxygen atoms combined in peroxidic form per 10 atoms of etheric oxygen contained.

By N.M.R. examination this polymeric product was shown to consist of polyether chains containing groups CF O- together with groups in a molar ratio between them of l :l.5.

The spectroscopic data also showed that about half of the -CF O units in the chain were in sequences of two or more of these units.

Groups of CF(CF )-O were. also present in the polyether chain in an amount corresponding to aboutv one such group per 20 groups 'C F 0--.

As regards the terminal groups, this polyether product was characterized by the presence of (l) CF O groups in three different forms of which the first one was prevailing, and also by the presence of (2) acid terminal groups of five types The gases leaving the reactor were washed with aqueous KOH solution, whereby it was determined that 156 g of C F had been converted by oxidative demolition according to the reaction I EXAMPLES 18 to 24 By using the same apparatus as described in the preceding example and by working analogously, a se-. ries of tests were carried out varying temperature and pressure of the reacting mixture.

The working conditions and the main data for the products obtained are reported in the following table. The characteristics of the polymeric products were obtained from experimental analytical results while the ratios relating to the various structural units contained in the polymeric chain were evaluated by examination of the N.M.R. spectrum, on the basis of the aforementioned criteria.

Example 24 is reported only for the sake of comparison. Thus, it shows that when the photochemical oxidation is carried out at low temperatures, and more particularly 'at temperatures of about 55 or below, the polymeric chain forming the oily polyether product contains virtually no units of the type -CF O and TABLE 3 Example No. 18 19 20 Reaction conditions temp C absolute pressure ,atm 7 7 5 initial C l- 22m 24 +2 to+2 lto12 CFLBBOOAB ms msu r.9e o.su

(Q+R)/P 0.72 0.28 0.55 R 0.08 0.10 0.10 S/(P+Q+R+1) 0.08 0.17 0.11 Prevailing structure ofA COF COF COF -CF,-COF CB-COF CECOF CFCOF CF-COF CF-COF Fa dlFs 1 3 21 22 23 24 2 to +2 -2 to +1 8 to 5 60 to 55 5 3 3 l 1060 1070 1065 1040 2 2 2 2 As will be apparent, changes and variations can be made in details, in practicing this invention, without de- I parting from the spirit thereof.

We claim: l. A linear perfluorinated polyether consisting of at least one repeating unit selected from the group consisting of and CF O units, said repeating units being linked one to another either directly or through an 0.xygen atom in which latter case thereis a peroxy linkage, the sum of the repeating units present along the chain being from 1 to 100, the ratio of the sum of the total CF -O units and total units to the total C F -O- units being from zero to 2, and the ratio of total active peroxidic oxygen units to the total --C F --O units being from zero to 1, said chain containing at least one C F O- unit and having as terminal groups at one end a CF O-- radical linked to said chain through a carbon atom and at the other end a COF radical linked to said chain through a non-peroxidic oxygen atom.

2. The perfluorinated polyether of claim 1, wherein the ratio of the sum of the total CF -O units and the total units to the total C F -O units is from 0.03 to 1.

3. The perfluorinated polyether of claim 1, said polyether having the formula CF O--(C F O) COF wherein P is an integer from 1 through 5.

4. The perfluorinated polyether of claim 1, said polyether having the formula wherein Pfifibfif .5. The perfluorinated polyether of claim 1, said polyether having the formula wherein P is l, 2 or 3.

v UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 699 145 Dated OCtObeT 1 7 1972 Dario Sianesi et a1. Inventor(s) It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

Title Page, Title: FLUORINATED OXYGEN-CONTAINING PRODUCTS AND PROCESS FOR PREPARATION THEREOF" should read PERFLUORINATED LINEAR POLYETHE RS Column 21, line 47, product," should read product;

iiigned and sealed this 31st day of December 1974.

(SEAL) Attest:

MCCOY M. GIBSONIJR. c MARSHALL DANN Attesting Officer Commissioner of Patents FORM PO-1050 (10-69) USCOMM-DC 60376-P69 U.S GOVERNMENT PRINTING OFFICE: 869- 930 

2. The perfluorinated polyether of claim 1, wherein the ratio of the sum of the total -CF2-O- units and the total units to the total -C3F6-O- units is from 0.03 to
 1. 3. The perfluorinated polyether of claim 1, said polyether having the formula CF3-O-(C3F6- O)-PCOF wherein P is an integer from 1 through
 5. 4. The perfluorinated polyether of claim 1, said polyether having the formula wherein P is 1, 2 or
 3. 5. The perfluorinated polyether of claim 1, said polyether having the formula wherein P is 1, 2 or
 3. 